Resultats de la cerca - Bai-Lin Wu
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Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis per Irene Mademont‐Soler, Carmen Morales, Anna Soler, J. M. Martínez‐Crespo, Yinchen Shen, Ester Margarit, Núria Clusellas, María Obón, Bai‐Lin Wu, Aurora Sánchez
Publicat 2012Artigo -
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Global DNA hypomethylation is associated with NTD‐affected pregnancy: A case‐control study per Xiaoli Chen, Jin Guo, Yunping Lei, Jizhen Zou, Xiaolin Lü, Yihua Bao, Lihua Wu, Jianxin Wu, Xiaoying Zheng, Yiping Shen, Bai‐Lin Wu, Ting Zhang
Publicat 2010Artigo -
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Border-zone cardiomyocytes and macrophages regulate extracellular matrix remodeling to promote cardiomyocyte protrusion during cardiac regeneration per Florian Constanty, Bai‐Lin Wu, Ke-Hsuan Wei, I-Ting Lin, Julia Dallmann, Stefan Günther, Till Lautenschlaeger, Rashmi Priya, Shih-Lei Lai, Didier Y. R. Stainier, Arica Beisaw
Publicat 2025Artigo -
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Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development per Thị Kim Tuyền Đặng, Wenfeng Duan, Bin Yu, Dali Tong, Connie Cheng, Y F Zhang, Weiwei Wu, K Ye, W X Zhang, Meng Wu, Bai-Lin Wu, Yu An, Zilong Qiu, Bo Wu
Publicat 2017Artigo -
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SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss per Pu Dai, Qi Li, Deliang Huang, Yongyi Yuan, Dongyang Kang, David T. Miller, Hong Shao, Qingwen Zhu, Jia He, Fei Yu, Xin Liu, Bing Han, Huijun Yuan, Orah S. Platt, Dongyi Han, Bai-Lin Wu
Publicat 2008Artigo -
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Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation per Bixia Xiang, Hongbo Zhu, Yiping Shen, David T. Miller, Kangmo Lu, Xiao Hu, Hans C. Andersson, Tarachandra M. Narumanchi, Yueying Wang, José E. Martínez, Bai-Lin Wu, Peining Li, Marilyn M. Li, Tian-Jian Chen, Yao‐Shan Fan
Publicat 2010Artigo -
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Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions per Andrew Dauber, Yongguo Yu, Michael C. Turchin, Charleston W. K. Chiang, Yan Meng, Ellen W. Demerath, Sanjay R. Patel, Stephen S. Rich, Jerome I. Rotter, Pamela J. Schreiner, James Wilson, Yiping Shen, Bai-Lin Wu, Joel N. Hirschhorn
Publicat 2011Artigo -
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Homozygous <i>PLCB1</i> deletion associated with malignant migrating partial seizures in infancy per Annapurna Poduri, Sameer S. Chopra, Edward Neilan, Princess C. Elhosary, Manju A. Kurian, Esther Meyer, Brenda J. Barry, Omar Khwaja, Mustafa A. Salih, Tommy Stödberg, Ingrid E. Scheffer, Eamonn R. Maher, Mustafa Şahin, Bai‐Lin Wu, Gerard T. Berry, Christopher A. Walsh, Jonathan Picker, Sanjeev V. Kothare
Publicat 2012Artigo -
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Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies per Shuhua Xu, Xianyong Yin, Shilin Li, Wenfei Jin, Haiyi Lou, Ling Yang, Xiaohong Gong, Hongyan Wang, Yiping Shen, Xuedong Pan, Yungang He, Yajun Yang, Yi Wang, Wenqing Fu, Yu An, Jiucun Wang, Jingze Tan, Ji Qian, Xiaoli Chen, Xin Zhang, Yangfei Sun, Xuejun Zhang, Bai-Lin Wu, Jin Li
Publicat 2009Artigo -
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Association between Microdeletion and Microduplication at 16p11.2 and Autism per Lauren A. Weiss, Yiping Shen, Joshua M. Korn, Dan E. Arking, David T. Miller, Ragnheiður Fossdal, Evald Sæmundsen, Hreinn Stefánsson, Todd Green, Orah S. Platt, Douglas M. Ruderfer, Christopher A. Walsh, David Altshuler, Aravinda Chakravarti, Rudolph E. Tanzi, Hreinn Stefánsson, Susan L. Santangelo, James F. Gusella, Pamela Sklar, Bai-Lin Wu, Mark J. Daly
Publicat 2008Artigo
Eines de cerca:
Matèries relacionades
Biology
Genetics
Gene
Medicine
Internal medicine
Psychiatry
Genome
Mutation
Phenotype
Psychology
Autism
Copy-number variation
Genotype
Neuroscience
Allele
Autism spectrum disorder
Population
Single-nucleotide polymorphism
Cell biology
Endocrinology
Evolutionary biology
Gene expression
Pregnancy
Allele frequency
Audiology
Chemistry
Chromosome
Cohort
Embryo
Environmental health